[Preventive effect of KZ-1026 on acute liver injury induced by CCl4 in rats: histochemical, enzyme-histochemical and ultrastructural studies]

Nihon Yakurigaku Zasshi. 1989 Jan;93(1):17-27. doi: 10.1254/fpj.93.17.
[Article in Japanese]

Abstract

The preventive effect of KZ-1026 on acute liver injury induced by CCl4 in rats was evaluated histochemically, enzyme-histochemically and ultrastructurally. Rats that received 50% CCl4 (2 ml/kg) intraperitoneally were sacrificed at 3, 7 and 24 hr. Remarkable reductions in hepatic glycogen, RNA and G-6-Pase activity were observed in the centrilobular area at 3 hr, and ballooned cells appeared in the mid-zone at 7 hr. At 24 hr, the above histochemical parameters in the hepatocytes of the centrilobular area and mid-zone were extensively reduced, while the number of ballooned cells in the mid-zone was increased. KZ-1026 (200 mg/kg) was given orally at 24 and 4 hr before, simultaneously with or 3 hr after CCl4 treatment, and each rat was sacrificed at 24 hr after CCl4 administration. Pretreatment with KZ-1026 24 hr before CCl4 administration prevented reduction of RNA, glycogen and G-6-Phase activity, as well as disruption of rER and proliferation of sER due to CCL4 toxicity. This preventive effect of KZ-1026 was reduced by posttreatment; however, only the decrease in cytoplasmic RNA was well prevented. These results suggested that KZ-1026 is protective against CCl4-induced acute liver injury.

MeSH terms

  • Acute Disease
  • Animals
  • Carbon Tetrachloride Poisoning / metabolism
  • Carbon Tetrachloride Poisoning / pathology
  • Carbon Tetrachloride Poisoning / prevention & control*
  • Chemical and Drug Induced Liver Injury / metabolism
  • Chemical and Drug Induced Liver Injury / pathology
  • Chemical and Drug Induced Liver Injury / prevention & control*
  • Endoplasmic Reticulum / ultrastructure
  • Glucose-6-Phosphatase / metabolism
  • Histocytochemistry
  • Ketones / therapeutic use*
  • Liver / enzymology
  • Liver / metabolism
  • Liver / ultrastructure
  • Liver Glycogen / metabolism
  • Male
  • Microscopy, Electron
  • RNA / metabolism
  • Rats
  • Rats, Inbred Strains
  • Thiophenes / therapeutic use*

Substances

  • Ketones
  • Liver Glycogen
  • Thiophenes
  • RNA
  • 2-(1,3-dithiolan-2-ylidene)-1-phenyl-1,3-butanedione
  • Glucose-6-Phosphatase